一例门诊护理中头孢曲松诱发的免疫性溶血性贫血病例

Q3 Medicine
Rakhee Mistry , Luke S.P. Moore , Nabeela Mughal , Andrew Godfrey , Stephen Hughes
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引用次数: 0

摘要

背景药物诱发免疫性溶血性贫血(DIIHA)是一种罕见的不良反应,其程度从轻微到致命不等(Garratty,2010 年)。据报道,导致严重免疫性溶血性贫血最常见的一类药物是第二代和第三代头孢菌素(如头孢曲松)(Garratty,2010年;Hill等人,2017年)、我们报告了一起通过门诊肠外抗菌治疗(OPAT)服务在非卧床环境下为患者注射头孢曲松而导致的严重、危及生命的 DIIHA 事件,以及我们随后对该不良反应的处理。他在非卧床护理病房开始接受头孢曲松治疗,每天静脉注射 4 克。在接受第九次输液后不久,他的脸色急剧苍白、心动过速、呼吸急促、血压过低,并在病房内多次目睹晕厥发作。血气检测血红蛋白水平降至 30 克/升,正式实验室分析(雅培® Alinity)结果为 39 克/升(基线为 97 克/升)。治疗包括大剂量皮质类固醇和单剂量静脉注射免疫球蛋白。随即停用头孢曲松,并开始使用不含β-内酰胺的治疗方案。结论:我们的病例突出表明,门诊护理和 OPAT 团队需要注意这种罕见的特异性不良反应,它可能发生在临床病情稳定的患者身上。我们主张每周对 OPAT 患者进行血液监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of ceftriaxone-induced immune haemolytic anaemia in an ambulatory care setting

Background

Drug-induced immune haemolytic anaemia (DIIHA) is a rare adverse effect which varies between mild to fatal (Garratty, 2010). One of the most common class of drugs reported to cause severe DIIHA are the second and third generation cephalosporins (e.g. ceftriaxone) (Garratty, 2010, Hill et al., 2017).

We report an event of severe, life-threatening DIIHA caused by ceftriaxone administered in an ambulatory setting to a patient via Outpatient Parenteral Antimicrobial Therapy (OPAT) service and our subsequent management of the adverse reaction.

Case report

A 60-year old male was referred to the OPAT service for radiologically-confirmed osteomyelitis. He was commenced on ceftriaxone 4 g daily intravenous infusions in the ambulatory care unit. Shortly after receiving the ninth dose, he became acutely pale, tachycardic, tachypnoeic, and hypotensive with multiple witnessed syncopal episodes inside the unit. Haemoglobin level fell to <30 g/L on blood gas and on formal laboratory analysis (Abbott® Alinity) 39 g/L (from baseline of 97 g/L). No obvious source of bleeding was identified which suggested an acute haemolytic process.

Management included high-dose corticosteroids and a single dose of intravenous immunoglobulin. Ceftriaxone was immediately discontinued and a beta-lactam free regimen was commenced. Haemoglobin level improved within 24 h with a gradual return to baseline within seven days.

Conclusions

Our case highlights the need for ambulatory care and OPAT teams to be aware of this rare, idiosyncratic adverse reaction which may occur in otherwise clinically stable patients. We advocate weekly haematological monitoring in OPAT patients.

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来源期刊
Clinical Infection in Practice
Clinical Infection in Practice Medicine-Infectious Diseases
CiteScore
2.10
自引率
0.00%
发文量
95
审稿时长
82 days
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